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11 OMIM references -
12 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
9 OMIM references -
9 associated genes
No signs/symptoms info
MODY syndrome
Zonular cataract

ABCC8 CRYAA
BLK CRYAB
CEL CRYBA1
GCK CRYBA4
HNF1A CRYGB
HNF4A CRYGC
INS CRYGD
KCNJ11 HSF4
KLF11 MIP
NEUROD1
PAX4
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
INS
(0.49)
CRYAB



Citations in the biomedical literature:


MODY syndrome
ABCC8 BLK CEL GCK HNF1A HNF4A
INS KCNJ11 KLF11 NEUROD1 PAX4 PDX1

Zonular cataract
CRYAA CRYAB CRYBA1 CRYBA4 CRYGB CRYGC
CRYGD HSF4 MIP



MODY syndrome
Zonular cataract

Synonym(s):
- Maturity-onset diabetes of the young

Synonym(s):
- Lamellar cataract

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
11 OMIM references -
No MeSH references
External references:
9 OMIM references -
1 MeSH reference: C535342

No signs/symptoms info available.